The QC LIMS Administrator supports the Laboratory Information Management System in the QC department, managing data related to cell therapy and ensuring compliance within a GMP environment.

The Quality Control Analyst conducts QC testing, prepares reports, investigates discrepancies, and supports regulatory compliance for cell therapy products.

The Principal SAP Technical Architect will be responsible for the design, development, and support of SAP systems in a GMP environment, engaging in ABAP programming, Fiori development, and integration with middleware platforms while collaborating with cross-functional teams.

Lead the technical transfer of a mechanical system to a contract manufacturer, while managing design and ensuring manufacturability. Requires 15+ years experience in mechanical engineering.

The Project Manager will lead SAP implementation projects in GMP-regulated environments, overseeing project lifecycles, compliance, and cross-functional collaboration within biotech operations.

The SAP Finance Systems Product Owner will optimize finance processes within SAP in a regulated biotech environment, ensuring compliance and integration across various systems.

Lead and support the optimization of SAP Supply Chain processes in a GMP-regulated environment, ensuring compliance and efficient operations across various functions.

The Senior Quality Engineer ensures compliance with quality standards in an FDA-regulated environment, leading quality assurance for product development and manufacturing of advanced cell therapies.

The Automation Scientist will develop and optimize lab automation systems, manage QC method requirements, validate assays, and troubleshoot automation issues.

The Logistics Specialist oversees logistics and distribution systems, ensuring timely materials delivery and compliance with regulations. This hands-on role requires continuous improvement in efficiency and cost-effectiveness.

The Automation Engineer will develop and optimize lab automation systems, validate QC workflows, and ensure functionality of automated systems for cell therapy manufacturing.

The Marketing Coordinator manages logistics for conferences, supports digital marketing initiatives, and collaborates on content generation and marketing campaigns.

The Director of Enterprise Programs leads client programs in process development, managing teams, overseeing tech transfer, ensuring compliance, and optimizing manufacturing processes for cell therapies.

The Scientist in Analytical Development will advance analytical methods for cell-based therapies, support method transfer, train analysts, ensure compliance, and maintain high analytical operation standards while collaborating with multiple departments.

The Senior Systems Integration Engineer will lead system characterization, integration, troubleshooting, and continuous improvement of cell therapy manufacturing systems, collaborating with various teams and driving tasks to completion.

Lead the development of control systems for cell therapy manufacturing by designing, implementing, testing hardware controls, and collaborating across teams.

The Process Engineer will support automated cell therapy manufacturing processes, collaborating across teams to design, validate, and optimize efficient workflows and documentation.